FDA 510(k) Application Details - K072024

Device Classification Name	Set, Tubing, Blood, With And Without Anti-Regurgitation Valve   More FDA Info for this Device
510(K) Number	K072024
Device Name	Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
Applicant	NIPRO MEDICAL CORP. 3150 NW 107 AVE.. MIAMI, FL 33172 US Other 510(k) Applications for this Company
Contact	JESSICA OSWALD Other 510(k) Applications for this Contact
Regulation Number	876.5820   More FDA Info for this Regulation Number
Classification Product Code	FJK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/24/2007
Decision Date	10/04/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review